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Publication : italian journal of pediatrics
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Academic Journal

A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report

Subjects: ETF; ETFDH; Glutaric aciduria type II

  • Source: Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-5 (2022)

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Academic Journal

Cyclic vomiting syndrome in children: a nationwide survey of current practice on behalf of the Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) and Italian Society of Pediatric Neurology (SINP)

Subjects: Cyclic vomiting; Management; Outcomes

  • Source: Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-9 (2022)

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Academic Journal

A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report.

Subjects: GENETIC mutation; AMINO acid metabolism disorders; GENETIC testing

  • Source: Italian Journal of Pediatrics; 9/5/2022, Vol. 48 Issue 1, p1-5, 5p

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Academic Journal

Cyclic vomiting syndrome in children: a nationwide survey of current practice on behalf of the Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) and Italian Society of Pediatric Neurology (SINP).

  • Authors : Isoldi S; Maternal and Child Health Department, Santa Maria Goretti Hospital, Sapienza-University of Rome, Latina, Italy.; Di Nardo G

Subjects: Child Nutrition Sciences* ; Gastroenterology* ; Health Care Surveys* Familial cyclic vomiting syndrome

  • Source: Italian journal of pediatrics [Ital J Pediatr] 2022 Aug 30; Vol. 48 (1), pp. 156. Date of Electronic Publication: 2022 Aug 30.Publisher: BioMed Central Country of Publication: England NLM ID: 101510759 Publication Model: Electronic Cited Medium: Internet ISSN: 1824-7288

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